{
    "disease_id": "DOID:3490", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008104", 
            "name": "Noonan syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008104", 
            "name": "Turner phenotype with Normal karyotype"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008104", 
            "name": "female pseudo-Turner syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008104", 
            "name": "Noonan syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008104", 
            "name": "Male Turner syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008104", 
            "name": "pterygium colli syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008104", 
            "name": "Noonan syndrome 1; NS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008104", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008104", 
            "name": "NS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3490", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3490", 
            "name": "Turner's phenotype, karyotype normal"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3490", 
        "description": "A RASopathy that is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3490", 
        "name": "Noonan syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/3490#disease-associations", 
            "id": "3490", 
            "database": "Alliance of Genome Resources"
        }
    ]
}